TRICYCLIC CONDENSED HETEROCYCLIC COMPOUND, METHOD FOR PRODUCING SAME, AND USE THEREOF

Description

TECHNICAL FIELD

[0001] The present invention relates to a novel tricyclic condensed heterocyclic compound, a process of producing the same, and use thereof. The tricyclic condensed heterocyclic compound of the present invention has an inhibitory activity on growth of cancer cells and is useful as a pharmaceutical, especially as an antitumor agent.

BACKGROUND ART

[0002] As a result of past intensive studies, many compounds having an antitumor activity have been put into practical use. Anticancer agents that are currently used in clinical practice show temporary regression and disappearance of cancer, but they also have non-selective toxicity to normal cells, causing serious adverse effects; thus, use thereof is restricted. Further, inherently resistant cancer against which an anticancer agent is not effective and acquisition of resistance to an anticancer drug which is found mainly in cases of recurrence have also been clinical problems. Under such circumstances, creation of a new antitumor agent has still been desired.

[0003] It is known that many actinomycetes are capable of producing an antibiotic. Hence, the search for a novel compound derived from an actinomycete has widely been conducted.

SUMMARY OF INVENTION

TECHNICAL PROBLEMS

[0004] The present invention is aimed at finding a novel substance derived from a natural source and providing a novel compound having an antitumor activity.

SOLUTION TO PROBLEMS

[0005] As a result of the search for a novel compound from a culture fluid of an actinomycete belonging to the genus Streptomyces, the present inventors found compounds having a novel framework. The present inventors determined the activity of these compounds and found that the compounds had an inhibitory activity on cell growth of tumor cells. By the above findings, the present invention was completed. The present invention is as described in the appended claims. Disclosed herein are items (1) to (14) below.

(1) A compound represented by any one of formulas (I), (II) and (III)





or an optical isomer thereof or a pharmaceutically acceptable salt thereof,
wherein R¹, R², R⁵ and R⁶ each independently represent a hydrogen atom, a methyl group, a hydroxymethyl group, a hydroxyl group, or represent a double bond by which R¹ and R² or R⁵ and R⁶ are bonded; R³, R⁴, R⁷ and R⁸ each independently represent a methyl group or a hydroxymethyl group; and R⁹ represents a hydrogen atom or a hydroxyl group.

(2) The compound of (1) represented by any one of formulas (IV), (V) and (VI)





or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein R⁵ and R⁶ each independently represent a hydrogen atom, a methyl group, a hydroxymethyl group or a hydroxyl group; R³, R⁴, R⁷ and R⁸ each independently represent a methyl group or a hydroxymethyl group; and R⁹ represents a hydrogen atom or a hydroxyl group.

(3) The compound of (2) represented by formula (IV) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein each of R³, R⁴, R⁵, R⁶, R⁷ and R⁸ is a methyl group.

(4) The compound of (2) represented by formula (IV) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein R³ is a hydroxymethyl group, and each of R⁴, R⁵, R⁶, R⁷ and R⁸ is a methyl group.

(5) The compound of (2) represented by formula (IV) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein R⁴ is a hydroxymethyl group, and each of R³ R⁵, R⁶, R⁷ and R⁸ is a methyl group.

(6) The compound of (2) represented by formula (IV) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein R⁵ is a hydroxymethyl group, and each of R³, R⁴, R⁶, R⁷ and R⁸ is a methyl group.

(7) The compound of (2) represented by formula (IV) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein R⁶ is a hydroxymethyl group, and each of R³, R⁴, R⁵, R⁷ and R⁸ is a methyl group.

(8) The compound of (2) represented by formula (V) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein R⁹ is a hydroxyl group, and each of R³, R⁵, R⁶, R⁷ and R⁸ is a methyl group.

(9) A pharmaceutical composition comprising as an active ingredient the compound of any one of (1) to (8) or an optical isomer thereof or a pharmaceutically acceptable salt thereof.

(10) The pharmaceutical composition of (9) which is an antitumor agent.

(11) A process of producing the compound of any one of (1) to (8), comprising: culturing a microorganism capable of producing the compound of any one of (1) to (8); and isolating the compound of any one of (1) to (8) from a product of the culturing.

(12) The process of (11), wherein the microorganism capable of producing the compound of any one of (1) to (8) is a microorganism which belongs to the genus Streptomyces.

(13) The process of (11), wherein the microorganism capable of producing the compound of any one of (1) to (8) is Streptomyces sp. NPS643 or a variant thereof.

(14) A process of producing a compound represented by formula (VII)

or an optical isomer thereof or a pharmaceutically acceptable salt thereof, comprising deriving a compound represented by formula (VII) or an optical isomer thereof or a pharmaceutically acceptable salt thereof from the compound of any one of (1) to (8) or an optical isomer thereof or a pharmaceutically acceptable salt thereof used as a starting material, wherein R¹, R⁴, R⁷, R¹⁰, R¹¹ and R¹³ are each independently and arbitrarily selected from - CH₂OH, -CH₂O-lower alkyl, -CH₂NH₂, -CH₂NH-lower alkyl, -CH₂N(lower alkyl)₂, -CH₂-halogen, -COOH, -CO₂-alkyl, -CONH₂ and COH; R² and R³ are arbitrarily selected from combinations of (hereinafter, a halogen is referred to as "X") (X,X), (H,X), (H,OH), (OH,H) and (H,NH₂) (the substituents in the parentheses may be in any order) and an epoxy in which R² and R³ are bonded to -O-; R⁵ and R⁶, R⁸ and R⁹, and R¹² and R¹⁴ are each independently and arbitrarily selected from combinations of (X,X), (H,X), (H,OH), (OH,X) and (H,NH₂) (the substituents in the parentheses may be in any order) and an epoxy in which R⁵ and R⁶, R⁸ and R⁹, or R¹² and R¹⁴ are bonded to -O-; and bonds indicated with a to f are each independently a single bond or a double bond.

ADVANTAGEOUS EFFECTS OF INVENTION

[0006] The compounds of the present invention are a compound having a novel framework and having an inhibitory activity on growth of cancer cells; thus, a novel anticancer agent can be provided.

DESCRIPTION OF EMBODIMENTS

[0007] As used herein, the term "halogen group" refers to a group of any one of fluorine, chlorine, bromine and iodine.

[0008] As used herein, the term "lower alkyl group" refers to, for example, a linear or branched C_1-6 alkylgroup. As a C_1-6 alkyl group, for example, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, tert-butyl, n-pentyl, n-hexyl or the like is used.

[0009] As a salt of the compounds of the present invention, a pharmaceutically or physiologically acceptable acid addition salt is especially preferred. Examples of such a salt that can be used include a salt of an inorganic acid (e.g., hydrochloric acid, phosphoric acid, hydrobromic acid, sulfuric acid); a salt of an organic acid (e.g., acetic acid, formic acid, propionic acid, fumaric acid, maleic acid, succinic acid, tartaric acid, lactic acid, citric acid, malic acid, oxalic acid, benzoic acid, methanesulfonic acid, p-toluenesulfonic acid, benzenesulfonic acid); and a salt of an alkali (e.g., sodium, potassium, magnesium, calcium, ammonium, pyridine, triethylamine).

[0010] A process of producing a compound of the present invention will be described below.

[0011] A compound of the present invention can be obtained by culturing bacteria which are capable of producing the compound and belong to the genus Streptomyces, and extracting the compound from the culture fluid and purifying it by a commonly-used method. Examples of bacteria which are capable of producing the compound and belong to the genus Streptomyces include Streptomyces sp. NPS643.

[0012] Streptomyces sp. NPS643 is a new strain separated from the ocean. As a result of analysis of the amino acid composition of a cell wall by methods of Uchida (Biseibutsu no kagakubunruijikkenho (Method for the microbial chemotaxonomy and experiment), p. 5-45, Japan Scientific Societies Press, 1982) and Suzuki (Hosenkin no bunri to dotei (Isolation and identification of actinomycete), p. 50-55, Business Center for Academic Societies Japan, 2001), glutamic acid, glycine, alanine and LL-diaminopimelic acid were detected; thus, the type of the cell wall was inferred as Type I. The major menaquinone of the bacterial body was extracted by a method of Nishijima et al. (J. Microbiol. Methods, 28, p. 113-122,1997), and the attribution of the quinone molecular species was determined by a method of Yamada et al. (Biseibutsu no kagakubunruijikkenho (Method for the microbial chemotaxonomy and experiment), p. 143-155, Japan Scientific Societies Press, 1982); the results were MK-9(H4) and MK-9(H6). As a result of homology search of 16SrDNA sequence 1386bp of sp. NPS643 using BLAST, it was determined that the most closely related species were Streptomyces cacaoi subsp. cacaoi NBRC12748 (96.0%), Streptomyces albus subsp. albus DSM40313 (95.7%), Streptomyces gibsonii NBRC15415 (95.6%), Streptomyces rangoonensis NBRC13078 (95.6%) and Streptomyces violaceoruber KCTC9787 (95.6%). Further, by phylogenetic tree analysis it was determined that sp. NPS643 did not form any cluster with a known strain.

[0013] Accordingly, sp. NPS643 was determined as the genus Streptomyces and named Streptomyces sp. NPS643. It is to be noted that the deposit of the strain has been made with the International Patent Organism Depository, the National Institute of Advanced Industrial Science and Technology, under the accession number FERM BP-11109 (date of depositary: June 4, 2008).

Method of culturing bacteria capable of producing NPS643 substance

[0014] Bacteria capable of producing NPS643 substance which belongs to actinomycete are cultured in a culture medium containing nutrients that a normal microorganism can utilize. As a nutrient source, a publicly-known nutrient source that has conventionally been used in the culture of an actinomycete can be used. For example, as a carbon source, glucose, starch syrup, dextrin, starch, molasses, animal oil, vegetable oil, etc. can be used. As a nitrogen source, soybean meal, wheat germ, corn steep liquor, cottonseed meal, meat extract, peptone, yeast extract, ammonium sulfate, sodium nitrate, urea, etc. can be used. It is effective to add, as necessary, an inorganic salt capable of producing ions of sodium, potassium, calcium, magnesium, cobalt, chlorine, phosphoric acid, sulfuric acid, etc. Further, organic and inorganic substances which promote the growth of bacteria and the production of NPS643 substance may be added as appropriate. As to a culture method, a method of culturing under aerobic conditions is suitable. A suitable temperature for the culture is 25 to 30°C; in many cases, the culture is conducted at about 28°C. In either of shaking culture and tank culture, the accumulation of NPS643 substance produced reaches the maximum after, in general, 2 to 10 days, depending on the culture medium and culture conditions. When the amount of NPS643 substance accumulated in the culture reaches the maximum, the culture is stopped, and an intended substance is isolated from the culture fluid and purified.

[0015] Properties of sp. NPS643 tend to change easily, like other actinomycetes. For example, a mutant (spontaneous or induced), zygote or gene recombinant derived from sp. NPS643 can be used in the present invention, as long as it is capable of producing NPS643 substance.

[0016] A microorganism of Streptomyces other than sp. NPS643 can also be used as the bacteria capable of producing the compound of the present invention, as long as it is a microorganism capable of producing the compound of the present invention. By checking the culture fluid of the microorganism, it is possible to easily determine whether the microorganism is a microorganism capable of producing the compound of the present invention. The same applies to a microorganism other than those of the genus Streptomyces.

[0017] Like other actinomycetes, an actinomycete which belongs to the genus Streptomyces and is capable of producing the compound of the present invention can be mutated by, for example, irradiation with UV, X-rays, radiation or the like, single spore isolation, various mutation treatments or other means. Such a mutant or a spontaneous mutant is not substantially different in type from the strain described above in terms of taxonomical properties, and any of them capable of producing the compound of the present invention can be used in the process of the present invention.

[0018] To isolate the compound of the present invention from an actinomycete culture fluid, means of extraction and purification of actinomycete metabolites can be used. For example, the purification can be conducted by combining as appropriate or repeating column chromatography, ion exchange chromatography, high performance liquid chromatography, gel filtration chromatography, etc. using an organic solvent fraction, silica gel and ODS.

[0019] By using the compound of the present invention isolated from the above microorganism culture product as a material and chemically modifying the functional groups, a derivative can be synthesized using the compound of the present invention as an intermediate. Since reactive functional groups such as carboxylic acid, double bonds and hydroxyl groups are present in the compound of the present invention, the chemical modification can be conducted easily.

[0020] Examples of a method for the derivatization include publicly-known methods such as dihalogenation reaction or any equivalent reaction described in Jikken Kagaku Koza (Encyclopedia of Experimental Chemistry), 5th Ed., 13, edited by The Chemical Society of Japan, p. 355-356 and 420-422, addition reaction of hydrogen halide or any equivalent reaction described in Jikken Kagaku Koza (Encyclopedia of Experimental Chemistry), 5th Ed., 13, edited by The Chemical Society of Japan, p. 428-430, Brown hydroboration reaction or any equivalent reaction described in Jikken Kagaku Koza (Encyclopedia of Experimental Chemistry), 4th Ed., 20, edited by The Chemical Society of Japan, p. 75-76, hydroxymercuration-demercuration reaction or any equivalent reaction described in Comprehensive Organic Synthesis (1991), Vol. 4, p. 300-305, hydroxylation reaction via halogenated hydrin or any equivalent reaction described in Journal of Organic Chemistry, (2005), Vol. 70, p. 6721-6734, Brown hydroboration amination reaction described in Journal of American Chemical Society, (1964), Vol. 86, p. 3565-3566, and synthesis reaction of epoxide or any equivalent reaction described in Jikken Kagaku Koza (Encyclopedia of Experimental Chemistry), 4th Ed., 20, edited by The Chemical Society of Japan, p. 213-214.

[0021] Embodiments of the present invention will be described below. However, it is understood that the scope of the present invention is not limited by the Examples.

EXAMPLES

<Culture>

[0022] One platinum loop of Streptomyces sp. NPS643 which had been grown well in a culture medium prepared by adding 1.8% artificial sea water to Humic Acid-Vitamin agar (J. Ferment. Technol., 65, 501-509 (1987)) was inoculated into a liquid culture medium containing 3% soytone and 1.8% artificial sea water and shake cultured at 28°C at 200 rpm for 5 days. One milliliter was inoculated into 100 ml of liquid culture medium (2.5% glucose, 1.5% soytone, 0.2% yeast extract, 0.4% calcium carbonate and 1.8% artificial sea water, pH 7.2) in a 500-ml Erlenmeyer flask and cultured at 200 rpm for 6 days.

<Extraction>

[0023] Five liters of the culture fluid obtained by the above culture was divided into a supernatant and a bacterial body by centrifugal separation. The supernatant was extracted with 500 mL of ethyl acetate and 500 mL of butanol. The bacterial body was extracted with a mixed solution of methanol and ethanol and then filtered. The solvent was removed by concentration under reduced pressure to obtain a concentrate, and then the concentrate was dissolved in 200 mL of water and extracted with 200 mL of ethyl acetate and 200 mL of butanol. The organic layer was combined with the organic layer of the supernatant and then concentrated to obtain 9.75 g of residue. This residue was applied onto a column in which a chromatographic tube having a diameter of 7 cm was filled with 9 cm ODS (Fuji Silysia Chemical Ltd., DM1020T), and eluted with mixed solvents of water/methanol = 3/1, 1/1, 1/3 and 0/1 to obtain 400 ml fractions. Among these fractions, the water/methanol = 1/3 fraction was concentrated to obtain 401.2 mg of residue. This residue was applied onto a column in which a chromatographic tube having a diameter of 5 cm was filled with 14 cm silica gel (Kanto Chemical Co., Inc., silica gel 60N spherical, neutral, 40-50 mm), and developed with mixed solvents of chloroform/methanol = 1/0, 19/1, 9/1, 3/1, 1/1 and 0/1 to obtain fractions. Among these fractions, the chloroform/methanol = 9/1-3/1 fractions were concentrated to obtain 150.2 mg of residue. This residue was applied onto four TLC plates (Merck silica gel 60F₂₅₄ 20 × 10 cm) and developed with a mixed solvent of hexane/diethyl ether = 1/2. Separation was conducted using the UV absorption as an indicator, whereby Compounds 1 to 6 were isolated in amounts of 109.0 mg, 0.5 mg, 0.5 mg, 1.0 mg, 0.5 mg and 2.0 mg, respectively.

<Identification of compounds>

[0024] Physical properties of Compounds 1 to 6 thus isolated were as follows. The results of NMR spectra are shown in Table 1 (¹H NMR spectra (400 MHz, CD₃OD)) and Table 2 (¹³C NMR spectra (100 MHz, CD₃OD)). From this information, structures of Compounds 1 to 6 were determined as follows.

[0025] Compound 1

(1) Color and property: Colorless oil

(2) Molecular formula: C₂₂H₃₀O₃

(3) High resolution mass spectrometry (Waters LTC-remier XE)

Measured value: m/z 343.2270 (C₂₂H₃₀O₃+H⁺)

Theoretical value: m/z 343.2275

(4) Infrared absorption spectrum λ_max (KBr) cm^-1: 3431, 2964, 2925, 2860,1701,1655,1648, 1638, 1560, 1543, 1113

(5) Structural formula

[0026] Compound 2

(1) Color and property: Colorless oil

(2) Molecular formula: C₂₂H₃₀O₄

(3) High resolution mass spectrometry (Waters LTC-Premier XE)

Measured value: m/z 359.2227 (C₂₂H₃₀O₄+H⁺)

Theoretical value: m/z 359.2224

(4) Infrared absorption spectrum λ_max (KBr) cm^-1: 3422, 2967, 2929, 2870, 1645, 1559, 1454, 1398,1060

(5) Structural formula

[0027] Compound 3

(1) Color and property: Colorless oil

(2) Molecular formula: C₂₂H₃₀O₄

(3) High resolution mass spectrometry (Waters LTC-Premier XE)

Measured value: m/z 359.2224 (C₂₂H₃₀O₄+H⁺)

Theoretical value: m/z 359.2224

(4) Infrared absorption spectrum λ_max (KBr) cm^-1: 3421, 2968, 2923, 2869, 1637, 1560, 1458, 1394, 1314, 1087

(5) Structural formula

[0028] Compound 4

(1) Color and property: Colorless oil

(2) Molecular formula: C₂₂H₃₀O₄

(3) High resolution mass spectrometry (Waters LTC-Premier XE)

Measured value: m/z 359.2224 (C₂₂H₃₀O₄+H⁺)

Theoretical value: m/z 359.2224

(4) Infrared absorption spectrum λ_max (KBr) cm^-1: 3410, 2968, 2930, 2878, 1647, 1559, 1448, 1394,1314,1217,1085

(5) Structural formula

[0029] Compound 5

(1) Color and property: Colorless oil

(2) Molecular formula: C₂₂H₃₀O₄

(3) High resolution mass spectrometry (Waters LTC-Premier XE)

Measured value: m/z 351.2084 (C₂₂H₂₉O₃⁺)

Theoretical value: m/z 351.2038

(4) Infrared absorption spectrum λ_max (KBr) cm^-1: 3420, 2965, 2929, 2869, 1637, 1569, 1457, 1396, 1314, 1191, 1097, 1042

(5) Structural formula

[0030] Compound 6

(1) Color and property: Colorless oil

(2) Molecular formula: C₂₂H₃₀O₄

(3) High resolution mass spectrometry (Waters LTC-Premier XE)

Measured value: m/z 359.2223 (C₂₂H₃₀O₄+H⁺)

Theoretical value: m/z 359.2224

(4) Infrared absorption spectrum λ_max (KBr) cm^-1: 3420, 2970, 2926, 2870, 1647, 1559, 1448, 1397,1314,1251,1086,1033

(5) Structural formula

[Table 1]

Compound 1	Compound 2	Compound 3	Compound 4	Compound 5	Compound 6
δH, mult (J)	δH, mult (J)	δH, mult (J)	δH, mult (J)	δH, mult (J)	δH, mult (J)
4.02, s	3.97, s	4.11, s	4.01, s	4.12, s	4.02, s
5.19, s	5.17, s	5.19, s	5.19, s	5.22, s	5.15. s
2.27, s	2.62, s	2.27, s	2.27, s	2.29, s	2.37, s
5.61, s	5.68, s	5 68, s	5.64, s	5.66, s	4.51
4.10, s	4.07, s	4.26, s	4.10, s	4.22, s	4.14, s
0.84, s	0.82, s	0.85, s	0.86, s	0.79, s	0.82, s
1.66, s	1.69, s	1.70, s	1.67, s	1.64, s	1.65, s
1.25, s	3.37, 3.50 d (10.8)	1.29, s	1.23, s	1.22, s	1.28, s
1.81, s	1.83, s	4.13, 4.15, s	1.79, s	1.80, s	5.26, 5.06, s
1.19, s	1.19, s	1.17, s	1.18, s	1.22, s	1.18, s
6.97, d (15.9)	6.81, d (16.1)	6.87, d (16.0)	6.85, d (16.0)	6.85, d (160)	6.89, d (15.8)
5.83, d (15.9)	5.90, d (16.1)	5.85, d (16.0)	5.85, d (16.0)	5.86, d (16.0)	5.90, d (15.8)
5.49, d (6.3)	5.48, d (6.7)	5.49, d (6.2)	5.65, t (6.2)	5.70, d (6.2)	5.55, d (6.8)
1.64, d (6.3)	1.63, d (6.7)	1.63, d (6.2)	4.17, d (6.2)	1.77, d (6.2)	1.65, d (6.8)
1.59, s	1.57, s	1.58, s	1.63, s	3.95, 4.20, d (11.9)	1.64, s

[Table 2]

Compound 1	Compound 2	Compound 3	Compound 4	Compound 5	Compound 6
δC, H	δC, H	δC, H	δC, H	δC, H	δC, H
92.1, CH	91.2, CH	90.7, CH	90.9, CH	83.6, CH	90.3, CH
61.2, C	61.2, C	59.8, C	61.1, C	59.7, C	62.0, C
136.9, CH	136.4, CH	135.3, CH	136.9, CH	135.2, CH	135.4, CH
139.6, C	140.1, C	138.3, C	140.4, C	138.6, C	140.4, C
65.9, CH	58.7, CH	65.0, CH	65.7, CH	64.2, CH	66.1, CH
42.3, C	61.2, C	40.5, C	42.1, C	40.6, C	44.2, C
131.5, CH	128.1, CH	131.0, CH	131.6, CH	130.1, CH	80.3, CH
136.7, C	138.6, C	133.9, C	136.4, C	137.3, C	134.8, C
85.1, CH	84.4, CH	80.4, CH	85.0, CH	87.7, CH	85.7, CH
58.1, C	57.8, C	56.8, C	58.1, C	57.4, C	57.5, C
17.7, CH3	17.2, CH3	17.6, CH3	17.6, CH3	18.7, CH3	17.6, CH3
19.0, CH3	19.2, CH3	20.1, CH3	19.2, CH3	20.3, CH3	19.0, CH3
30.2, CH3	70.1, CH2	29.4, CH3	30.6, CH3	29.4, CH3	29. 1, CH3
20.7, CH3	20.7, CH3	63.1, CH2	20.4, CH3	22.3, CH3	120.0, CH3
26.6, CH3	26.2, CH3	25.1, CH3	27.8, CH3	25.5, CH3	28.0, CH3
153.7, CH	148.5, CH	149.5, CH	151.7, CH	150.4, CH	150.0, CH
123.7, CH	128.0, CH	128.5, CH	125.7, CH	120.0, CH	127.4, CH
174.2, C	175.7, C	174.2, C	175.8, C	174.5, C	175.8, C
135.2, C	138.6, C	138.2, C	136.3, C	135.5, C	134.8, C
120.3, CH	120.0, CH	118.7, CH	125.2, CH	123.3, CH	125.2, CH
12.9, CH3	12.9, CH3	12.9, CH3	59.1, CH2	15.9, CH3	12.9, CH3
14.4, CH3	14.3, CH3	15.7, CH3	14.7, CH3	56.7, CH2	14.2, CH3

<Pharmacological activity>

[0031] The cell growth inhibitory activity of Compound 1 was evaluated using 4 types of cancer cells. The cancer cells used were human cancer cells (HT-29, A431, NCI-H460, H-937). Compound 1 was dissolved in DMSO. One hundred milliliters of a suspension of cancer cells was charged in each 96 well micro plate (1.0 to 3.0 x 10³ cells/well). After 24 hours, each of solutions of Compounds 1 to 6 was added in an amount of 2 ml to 100 ml of culture fluid to give final concentrations of 3 mM, 1 mM, 0.3 mM, 0.1 mM and 0.03 mM and cultured for 72 hours. Thereafter, 20 ml of an Almar Blue reagent was added to each solution, followed by culturing for 6 hours. The growth inhibitory activity was measured by determining the fluorescence intensity with a multimicroplate reader (GENios plus microplate reader, Tecan) at a fluorescence wavelength of 590 nm and an excitation wavelength of 530 nm and calculating the IC₅₀ value for each cell by nonlinear regression analysis. The IC₅₀ value of cell growth inhibitory activity of Compound 1 is shown below.

[Table 3]

Cancer cell	HT-29	NCI-H460	U937	PC-3
IC50(µM)	0.59	0.58	1.10	0.82

[0032] The cell growth inhibitory activity of Compound 6 was evaluated using cancer cells (HT-29). The method for the evaluation was the same as the method by which Compound 1 was evaluated. The IC₅₀ value of cell growth inhibitory activity of Compound 6 was 0.31 µM.

INDUSTRIAL APPLICABILITY

[0033] The compounds of the present invention can provide a novel antitumor agent having an antitumor activity.

0-1	Form PCT/RO/134 (SAFE)
0-1-1	The indications relating to deposited microorganism or other biological material (PCT Rule 13bis) were made by:	JPO-PAS
		i171
0-2	International application number
0-3	Applicant's or agent's file reference	PCT2010-02
1	The indications made below relate to the deposited microorganism or other biological
1-1	material referred to in the description on: Paragraph number	0014
1-3	Identification of deposit
1-3-1	Name of depositary institution	International Patent Organism Depositary (IPOD), National Institute of Advanced Industrial Science and Technology (AIST)
1-3-2	Address of depositary institution	Tsukuba Central 6, 1-1, Higashi 1-chome, Tsukuba-shi, Ibaraki 305-8566 Japan
1-3-3	Date of deposit	June 4, 2008
1-3-4	Accession number	IPOD FERM BP-11109
1-5	Designated states for which indications are made	All designations

For receiving Office use only
0-4	This sheet was received with the international application (Yes/No)
0-4-1	Authorized officer

For International Bureau use only
0-5	This sheet was received by the International Bureau on:
0-5-1	Authorized officer

Claims

1. A compound represented by any one of formulas (IV), and (V)



or an optical isomer thereof or a pharmaceutically acceptable salt thereof,
wherein R⁵ and R⁶ each independently represent a hydrogen atom, a methyl group, a hydroxymethyl group or a hydroxyl group; R³, R⁴, R⁷ and R⁸ each independently represent a methyl group or a hydroxymethyl group; and R⁹ represents a hydrogen atom or a hydroxyl group.

2. The compound of Claim 1 represented by formula (IV) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein each of R³, R⁴, R⁵, R⁶, R⁷ and R⁸ is a methyl group.

3. The compound of Claim 1 represented by formula (IV) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein R³ is a hydroxymethyl group, and each of R⁴, R⁵, R⁶, R⁷ and R⁸ is a methyl group.

4. The compound of Claim 1 represented by formula (IV) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein R⁴ is a hydroxymethyl group, and each of R³, R⁵, R⁶, R⁷ and R⁸ is a methyl group.

5. The compound of Claim 1 represented by formula (IV) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein R⁵ is a hydroxymethyl group, and each of R³,R⁴, R⁶, R⁷ and R⁸ is a methyl group.

6. The compound of Claim 1 represented by formula (IV) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein R⁶ is a hydroxymethyl group, and each of R³, R⁴, R⁵, R⁷ and R⁸ is a methyl group.

7. The compound of Claim 1 represented by formula (V) or an optical isomer thereof or a pharmaceutically acceptable salt thereof, wherein R⁹ is a hydroxyl group, and each of R³ R⁵, R⁶ , R⁷ and R⁸ is a methyl group.

8. A pharmaceutical composition comprising as an active ingredient the compound of any one of Claims 1 to 7 or an optical isomer thereof or a pharmaceutically acceptable salt thereof.

9. A compound of any one of Claims 1 to 7 for use in the treatment of a tumor.

10. Use of a compound of any one of Claims 1 to 7 for the manufacture of a medicament for treating a tumor.

11. A process of producing the compound of any one of Claims 1 to 7, comprising: culturing a microorganism capable of producing the compound of any one of Claims 1 to 7; and isolating the compound of any one of Claims 1 to 7 from a product of the culturing, wherein the microorganism capable of producing the compound of any one of Claims 1 to 7 is a microorganism which belongs to the genus Streptomyces.

12. The process of Claim 11, wherein the microorganism capable of producing the compound of any one of Claims 1 to 7 is Streptomyces sp. NPS643 or a variant thereof.

13. A process of producing a compound represented by formula (VII)

or an optical isomer thereof or a pharmaceutically acceptable salt thereof, comprising deriving a compound represented by formula (VII) or an optical isomer thereof or a pharmaceutically acceptable salt thereof from the compound of any one of Claims 1 to 7 or an optical isomer thereof or a pharmaceutically acceptable salt thereof used as a starting material, wherein R¹ R⁴, R⁷, R¹⁰, R¹¹ and R¹³ are each independently and arbitrarily selected from -CH₂OH, -CH₂O-lower alkyl, -CH₂NH₂, -CH₂NH-lower alkyl, -CH₂N(lower alkyl)₂, - CH₂-halogen, -COOH, -CO₂-alkyl -CONH₂ and COH;
R² and R³ are arbitrarily selected from combinations of (hereinafter, a halogen is referred to as "X") (X,X), (H,X), (H,OH), (OH,H) and (H,NH₂) (the substituents in the parentheses may be in any order) and an epoxy in which R² and R³ are bonded to -O-;
R⁵ and R⁶, R⁸ and R⁹, and R¹² and R¹⁴ are each independently and arbitrarily selected from combinations of (X,X), (H,X), (H,OH), (OH,X) and (H,NH₂) (the substituents in the parentheses may be in any order) and an epoxy in which R⁵ and R⁶, R⁸ and R⁹, or R¹² and R¹⁴ are bonded to -O-; and
bonds indicated with a to f are each independently a single bond or a double bond.

Ansprüche

1. Eine Verbindung, dargestellt durch eine der Formeln (IV) und (V),



oder ein optisches Isomer davon oder ein pharmazeutisch verträgliches Salz davon, wobei R⁵ und R⁶ jeweils unabhängig voneinander ein Wasserstoffatom, eine Methylgruppe, eine Hydroxymethylgruppe oder eine Hydroxygruppe darstellen; R³, R⁴, R⁷ und R⁸ jeweils unabhängig voneinander eine Methylgruppe oder eine Hydroxymethylgruppe darstellen; und R⁹ ein Wasserstoffatom oder eine Hydroxygruppe darstellt.

2. Die Verbindung nach Anspruch 1, dargestellt durch Formel (IV), oder ein optisches Isomer davon oder ein pharmazeutisch verträgliches Salz davon, wobei jeder Rest R³, R⁴, R⁵, R⁶, R⁷ und R⁸ eine Methylgruppe ist.

3. Die Verbindung nach Anspruch 1, dargestellt durch Formel (IV), oder ein optisches Isomer davon oder ein pharmazeutisch verträgliches Salz davon, wobei R³ eine Hydroxymethylgruppe ist und jeder Rest R⁴, R⁵, R⁶, R⁷ und R⁸ eine Methylgruppe ist.

4. Die Verbindung nach Anspruch 1, dargestellt durch Formel (IV), oder ein optisches Isomer davon oder ein pharmazeutisch verträgliches Salz davon, wobei R⁴ eine-Hydroxymethylgruppe ist und jeder Rest R³, R⁵, R⁶, R⁷ und R⁸ eine Methylgruppe ist.

5. Die Verbindung nach Anspruch 1, dargestellt durch Formel (IV), oder ein optisches Isomer davon oder ein pharmazeutisch verträgliches Salz davon, wobei R⁵ eine Hydroxymethylgruppe ist und jeder Rest R³, R⁴, R⁶, R⁷ und R⁸ eine Methylgruppe ist.

6. Die Verbindung nach Anspruch 1, dargestellt durch Formel (IV), oder ein optisches Isomer davon oder ein pharmazeutisch verträgliches Salz davon, wobei R⁶ eine Hydroxymethylgruppe ist und jeder Rest R³, R⁴, R⁵, R⁷ und R⁸ eine Methylgruppe ist.

7. Die Verbindung nach Anspruch 1, dargestellt durch Formel (V), oder ein optisches Isomer davon oder ein pharmazeutisch verträgliches Salz davon, wobei R⁹ eine Hydroxygruppe ist und jeder Rest R³, R⁵, R⁶, R⁷ und R⁸ eine Methylgruppe ist.

8. Ein Arzneimittel, umfassend als einen Wirkstoff die Verbindung nach einem der Ansprüche 1 bis 7 oder ein optisches Isomer davon oder ein pharmazeutisch verträgliches Salz davon.

9. Eine Verbindung nach einem der Ansprüche 1 bis 7 zur Verwendung bei der Behandlung eines Tumors.

10. Verwendung einer Verbindung nach einem der Ansprüche 1 bis 7 zur Herstellung eines Medikaments zur Behandlung eines Tumors.

11. Ein Verfahren zur Herstellung der Verbindung nach einem der Ansprüche 1 bis 7, umfassend: Züchten eines Mikroorganismus, der zur Herstellung der Verbindung nach einem der Ansprüche 1 bis 7 imstande ist; und Isolieren der Verbindung nach einem der Ansprüche 1 bis 7 aus einem Züchtungsprodukt, wobei der Mikroorganismus, der zur Herstellung der Verbindung nach einem der Ansprüche 1 bis 7 imstande ist, ein Mikroorganismus ist, der zur Gattung Streptomyces gehört.

12. Das Verfahren nach Anspruch 11, wobei der Mikroorganismus, der zur Herstellung der Verbindung nach einem der Ansprüche 1 bis 7 imstande ist, Streptomyces sp. NPS643 oder eine Variante davon ist.

13. Ein Verfahren zur Herstellung einer Verbindung, dargestellt durch Formel (VII),

oder eines optischen Isomers davon oder eines pharmazeutisch verträglichen Salzes davon, umfassend Ableiten einer Verbindung, dargestellt durch Formel (VII), oder eines optischen Isomers davon oder eines pharmazeutisch verträglichen Salzes davon von der als Ausgangsmaterial verwendeten Verbindung nach einem der Ansprüche 1 bis 7 oder einem optischen Isomer davon oder einem pharmazeutisch verträglichen Salz davon, wobei R¹, R⁴, R⁷, R¹⁰, R¹¹ und R¹³ jeweils unabhängig voneinander und beliebig aus -CH₂OH, -CH₂O-Niederalkyl, -CH₂NH₂, -CH₂NH-Niederalkyl, -CH₂N(Niederalkyl)₂, -CH₂-Halogen, -COOH, -CO₂-Alkyl, -CONH₂ und COH ausgewählt sind;
R² und R³ beliebig aus den Kombinationen (nachstehend wird ein Halogenatom mit "X" bezeichnet) (X,X), (H,X), (H,OH), (OH,H) und (H,NH₂) (die Substituenten in Klammern können in beliebiger Reihenfolge auftreten) und einem Epoxy, wobei R² und R³ an -O-gebunden sind, ausgewählt sind;
R⁵ und R⁶, R⁸ und R⁹ und R¹² und R¹⁴ jeweils unabhängig voneinander und beliebig aus den Kombinationen (X,X), (H,X), (H,OH), (OH,X) und (H,NH₂) (die Substituenten in Klammern können in beliebiger Reihenfolge auftreten) und einem Epoxy, wobei R⁵ und R⁶, R⁸ und R⁹ oder R¹² und R¹⁴ an -O- gebunden sind, ausgewählt sind; und
Bindungen, die mit a bis f bezeichnet sind, unabhängig voneinander eine Einfachbindung oder eine Doppelbindung darstellen.

Revendications

1. Composé représenté par l'une quelconque des formules (IV) et (V) :



ou un isomère optique ou un sel pharmaceutiquement acceptable d'un tel composé, formules dans lesquelles chacun de R⁵ et R⁶ représente indépendamment un atome d'hydrogène, un groupe méthyle, un groupe hydroxyméthyle ou un groupe hydroxyle ; chacun de R³, R⁴, R⁷ et R⁸ représente indépendamment on groupe méthyle ou un groupe hydroxyméthyle ; et R⁹ représente un atome d'hydrogène ou un groupe hydroxyle.

2. Composé selon la revendication 1 représenté par la formule (IV) ou un isomère optique ou un sel pharmaceutiquement acceptable d'un tel composé, dans lequel chacun de R³, R⁴, R⁵, R⁶, R⁷ et R⁸ est un groupe méthyle.

3. Composé selon la revendication 1 représenté par la formule (IV) ou un isomère optique ou un sel pharmaceutiquement acceptable d'un tel composé, dans lequel R³ est un groupe hydroxyméthyle, et chacun de R⁴, R⁵, R⁶, R⁷ et R⁸ est un groupe méthyle.

4. Composé selon la revendication 1 représenté par la formule (IV) ou un isomère optique ou un sel pharmaceutiquement acceptable d'un tel composé, dans lequel R⁴ est un groupe hydroxyméthyle, et chacun de R³, R⁵, R⁶, R⁷ et R⁸ est un groupe méthyle.

5. Composé selon la revendication 1 représenté par la formule (IV) ou un isomère optique ou un sel pharmaceutiquement acceptable d'un tel composé, dans lequel R⁵ est un groupe hydroxyméthyle, et chacun de R³, R⁴, R⁶, R⁷ et R⁸ est un groupe méthyle.

6. Composé selon la revendication 1 représenté par la formule (IV) ou un isomère optique ou un sel pharmaceutiquement acceptable d'un tel composé, dans lequel R⁶ est un groupe hydroxyméthyle, et chacun de R³, R⁴, R⁵, R⁷ et R⁸ est un groupe méthyle.

7. Composé selon la revendication 1 représenté par la formule (V) ou un isomère optique ou un sel pharmaceutiquement acceptable d'un tel composé, dans lequel R⁹ est un groupe hydroxyle, et chacun de R³, R⁵, R⁶, R⁷ et R⁸ est un groupe méthyle.

8. Composition pharmaceutique comprenant, à titre d'agent actif, le composé de l'une quelconque des revendications 1 à 7 ou un isomère optique ou un sel pharmaceutiquement acceptable d'un tel composé.

9. Composé selon l'une quelconque des revendications 1 à 7, pour utilisation dans le traitement d'une tumeur.

10. Utilisation d'un composé selon l'une quelconque des revendications 1 à 7 pour la fabrication d'un médicament destiné au traitement d'une tumeur.

11. Procédé pour produire le composé selon l'une quelconque des revendications 1 à 7, comprenant : la culture d'un microorganisme capable de produire le composé de l'une quelconque des revendications 1 à 7 ; et l'isolation du composé de l'une quelconque des revendications 1 à 7 à partir d'un produit de la culture, dans lequel le microorganisme capable de produire le composé de l'une quelconque des revendications 1 à 7 est un microorganisme qui appartient au genre Streptomyces.

12. Procédé selon la revendication 11, dans lequel le microorganisme capable de produire le composé de l'une quelconque des revendications 1 à 7 est Streptomyces sp. NPS643 ou un variant de celui-ci.

13. Procédé pour produire un composé représenté par la formule (VII) :

ou un isomère optique ou un sel pharmaceutiquement acceptable d'un tel composé, comprenant la dérivation d'un composé représenté par la formule (VII) ou d'un isomère optique ou d'un sel pharmaceutiquement acceptable d'un tel composé à partir du composé de l'une quelconque des revendications 1 à 7 ou d'un isomère optique ou d'un sel pharmaceutiquement acceptable d'un tel composé, utilisé en tant que matériau de départ,
formule dans laquelle
chacun de R¹, R⁴, R⁷, R¹⁰, R¹¹ et R¹³ est indépendamment et arbitrairement choisi parmi -CH₂OH, -CH₂O-alkyle inférieur, -CH₂NH₂, -CH₂NH-alkyle inférieur, -CH₂N-(alkyle inférieur)₂, -CH₂-halogène, -COOH, -CO₂-alkyle, -CONH₂ et COH ;
R² et R³ sont arbitrairement choisis parmi les combinaisons suivantes (ci-après, un halogène est représenté par "X") : (X,X), (H,X), (H,OH), (OH,H) et (H,NH₂) (les substituants entre parenthèses pouvant être dans un ordre quelconque), et un époxy dans lequel R² et R³ sont liés à -O- ;
chacun de R⁵ et R⁶, R⁸ et R⁹, et R¹² et R¹⁴, est indépendamment et arbitrairement choisie parmi les combinaisons (X,X), (H,X), (H,OH), (OH,X) et (H,NH₂) (les substituants entre parenthèses pouvant être dans un ordre quelconque), et un époxy dans lequel R⁵ et R⁶, R⁸ et R⁹, ou R¹² et R¹⁴, sont liés à -O- ; et
chacune des liaisons indiquées par a à f est indépendamment une liaison simple ou une double liaison.